DE602004009089D1 - Pyrrolderivate mit antibakterieller wirkung - Google Patents
Pyrrolderivate mit antibakterieller wirkungInfo
- Publication number
- DE602004009089D1 DE602004009089D1 DE602004009089T DE602004009089T DE602004009089D1 DE 602004009089 D1 DE602004009089 D1 DE 602004009089D1 DE 602004009089 T DE602004009089 T DE 602004009089T DE 602004009089 T DE602004009089 T DE 602004009089T DE 602004009089 D1 DE602004009089 D1 DE 602004009089D1
- Authority
- DE
- Germany
- Prior art keywords
- antibacterial effect
- pyrrol derivatives
- pyrrol
- derivatives
- antibacterial
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0321509A GB0321509D0 (en) | 2003-09-13 | 2003-09-13 | Chemical compounds |
GB0321509 | 2003-09-13 | ||
GB0410527A GB0410527D0 (en) | 2004-05-12 | 2004-05-12 | Chemical compounds |
GB0410527 | 2004-05-12 | ||
PCT/GB2004/003874 WO2005026149A1 (en) | 2003-09-13 | 2004-09-10 | Pyrrol derivatives with antibacterial activity |
Publications (2)
Publication Number | Publication Date |
---|---|
DE602004009089D1 true DE602004009089D1 (de) | 2007-10-31 |
DE602004009089T2 DE602004009089T2 (de) | 2008-06-12 |
Family
ID=34315434
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE602004009089T Active DE602004009089T2 (de) | 2003-09-13 | 2004-09-10 | Pyrrolderivate mit antibakterieller wirkung |
Country Status (20)
Country | Link |
---|---|
US (1) | US7709503B2 (de) |
EP (1) | EP1664025B1 (de) |
JP (1) | JP4959329B2 (de) |
KR (1) | KR20070026318A (de) |
AR (1) | AR046160A1 (de) |
AT (1) | ATE373650T1 (de) |
AU (1) | AU2004272338B2 (de) |
BR (1) | BRPI0414330A (de) |
CA (1) | CA2538552A1 (de) |
DE (1) | DE602004009089T2 (de) |
ES (1) | ES2291934T3 (de) |
HK (1) | HK1091491A1 (de) |
IL (1) | IL174165A0 (de) |
IS (1) | IS8403A (de) |
MX (1) | MXPA06002847A (de) |
NO (1) | NO20061657L (de) |
RU (1) | RU2006112046A (de) |
TW (1) | TW200526626A (de) |
UY (1) | UY28510A1 (de) |
WO (1) | WO2005026149A1 (de) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2861070B1 (fr) * | 2003-10-17 | 2006-01-06 | Sanofi Synthelabo | Derives de n-[phenyl(pyrrolidin-2-yl)methyl]benzamide et n-[(azepan-2-yl)phenylmethyl]benzamide, leur preparation et leur application en therapeutique |
MY179032A (en) | 2004-10-25 | 2020-10-26 | Cancer Research Tech Ltd | Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors |
WO2006053227A2 (en) * | 2004-11-10 | 2006-05-18 | Synta Pharmaceuticals Corp. | Il-12 modulatory compounds |
KR101422432B1 (ko) * | 2005-02-18 | 2014-07-22 | 아스트라제네카 아베 | 항균성 피페리딘 유도체 |
EP1856103A2 (de) * | 2005-02-18 | 2007-11-21 | AstraZeneca AB | Pyrrolderivate als dna-gyrase- und topoisomeraseinhibitoren |
JP2008531673A (ja) * | 2005-03-04 | 2008-08-14 | アストラゼネカ アクチボラグ | 抗菌活性をもつアゼチジン及びピロールの三環式誘導体 |
US8796293B2 (en) | 2006-04-25 | 2014-08-05 | Astex Therapeutics Limited | Purine and deazapurine derivatives as pharmaceutical compounds |
WO2008020227A2 (en) * | 2006-08-17 | 2008-02-21 | Astrazeneca Ab | Antibacterial pyrrolecarboxamides |
TW200819437A (en) * | 2006-08-17 | 2008-05-01 | Astrazeneca Ab | Chemical compounds |
WO2008020229A2 (en) * | 2006-08-17 | 2008-02-21 | Astrazeneca Ab | Antibacterial pyrrolecarboxamides |
EP1903038A1 (de) * | 2006-09-07 | 2008-03-26 | Bayer Schering Pharma Aktiengesellschaft | N-(1-Hetaryl-piperidin-4-yl)-(het)arylamide als EP2-Rezeptor Modulatoren |
TW200906412A (en) * | 2007-06-12 | 2009-02-16 | Astrazeneca Ab | Piperidine compounds and uses thereof |
UY31384A1 (es) | 2007-10-11 | 2009-05-29 | Novedosos compuestos heterociclicos para la inhibicion de la proteina quinasa b | |
TWI498115B (zh) | 2007-12-27 | 2015-09-01 | Daiichi Sankyo Co Ltd | 咪唑羰基化合物 |
JP5524491B2 (ja) * | 2008-03-04 | 2014-06-18 | 石原産業株式会社 | 3−アミノ−2−クロロ−6−トリフルオロメチルピリジンの製造方法 |
TW201026694A (en) * | 2008-12-12 | 2010-07-16 | Astrazeneca Ab | Compound 468 |
TW201026695A (en) * | 2008-12-12 | 2010-07-16 | Astrazeneca Ab | Piperidine compounds and uses thereof-596 |
CN102264705A (zh) | 2008-12-24 | 2011-11-30 | 辛根塔有限公司 | 制备芳基酰胺的方法 |
TW201102065A (en) | 2009-05-29 | 2011-01-16 | Astrazeneca Ab | Heterocyclic urea derivatives and methods of use thereof |
TWI491606B (zh) | 2009-07-13 | 2015-07-11 | Gilead Sciences Inc | 調節細胞凋亡信號之激酶的抑制劑 |
WO2011024004A1 (en) | 2009-08-26 | 2011-03-03 | Astrazeneca Ab | Heterocyclic urea derivatives useful for treatment of bacterial infection |
JP2013503178A (ja) | 2009-08-26 | 2013-01-31 | サイリーン ファーマシューティカルズ インコーポレーティッド | タンパク質キナーゼ調節物質としての縮合キノリン |
AU2010333338A1 (en) | 2009-12-14 | 2012-08-02 | Merck Patent Gmbh | Sphingosine kinase inhibitors |
CN102770419A (zh) | 2010-02-22 | 2012-11-07 | 先正达参股股份有限公司 | 作为杀虫化合物的二氢呋喃衍生物 |
WO2012007500A2 (de) | 2010-07-15 | 2012-01-19 | Bayer Cropscience Ag | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
SG193505A1 (en) | 2011-04-01 | 2013-10-30 | Astrazeneca Ab | Therapeutic treatment |
WO2012143248A1 (en) * | 2011-04-19 | 2012-10-26 | Nerviano Medical Sciences S.R.L. | Substituted pyrimidinyl-pyrroles active as kinase inhibitors |
US20140343049A1 (en) | 2011-08-22 | 2014-11-20 | Syngenta Participations Ag | Dihydrofuran derivatives as insecticidal compounds |
WO2013079964A1 (en) | 2011-11-30 | 2013-06-06 | Astrazeneca Ab | Combination treatment of cancer |
AU2013204533B2 (en) | 2012-04-17 | 2017-02-02 | Astrazeneca Ab | Crystalline forms |
EP2818461A1 (de) | 2013-06-26 | 2014-12-31 | Lonza Ltd | Verfahren zur Herstellung von 6-Trifluormethylpyridin-3-Carboxylsäurederivaten aus 4,4,4-Trifluor-3-Oxobutanoylchlorid |
EP2821399A1 (de) | 2013-07-04 | 2015-01-07 | Lonza Ltd | Verfahren zur Herstellung von 6-Trifluormethylpyridin-3-Carboxyl-Säurederivaten aus 4,4,4-Trifluor-3-Oxobutanoylchlorid |
WO2015090224A1 (zh) | 2013-12-20 | 2015-06-25 | 中国人民解放军军事医学科学院毒物药物研究所 | 新型哌啶氨甲酰类化合物、制备方法及其用途 |
BR112016030358A2 (pt) | 2014-06-26 | 2018-07-17 | Lonza Ltd | Método para a preparação de 4-alcóxi-1, 1, 1, trifluorobut-3-en-2-onas a partir de 1,1,1- trifluoroacetona |
EP3233829B1 (de) * | 2014-12-18 | 2019-08-14 | Pfizer Inc | Pyrimidin und triazinderivate und deren verwendung als axl-inhibitoren |
US9586933B2 (en) | 2014-12-23 | 2017-03-07 | Gilead Sciences, Inc. | Processes for preparing ASK1 inhibitors |
AU2016330271B2 (en) | 2015-09-30 | 2020-04-30 | Daiichi Sankyo Company, Limited | Hydroxyalkyl thiadiazole derivatives |
SG11201900633XA (en) * | 2016-07-28 | 2019-02-27 | Idorsia Pharmaceuticals Ltd | Piperidine cxcr7 receptor modulators |
DK3538528T3 (da) | 2016-11-08 | 2021-02-15 | Bristol Myers Squibb Co | Pyrrolamider som alpha v-integrinhæmmere |
JP2020511457A (ja) | 2017-03-14 | 2020-04-16 | 第一三共株式会社 | ヒドロキシアルキルチアジアゾール誘導体のn−ホスホノキシメチルプロドラッグ |
KR20190133667A (ko) | 2017-03-24 | 2019-12-03 | 다이쇼 세이야꾸 가부시끼가이샤 | 2(1h)-퀴놀리논 유도체 |
KR20200084879A (ko) | 2017-11-07 | 2020-07-13 | 브리스톨-마이어스 스큅 컴퍼니 | 알파 v 인테그린 억제제로서의 피롤로피라진 유도체 |
AU2019212888B8 (en) | 2018-01-26 | 2024-01-04 | Idorsia Pharmaceuticals Ltd | Crystalline forms of the CXCR7 receptor antagonist (3s,4s)-1- cyclopropylmethyl-4-{[5-(2,4-difluoro-phenyl)-isoxazole-3-carbonyl]- amino}-piperidine-3-carboxylic acid (1-pyrimidin-2-yl-cyclopropyl)-amide |
WO2020048949A1 (en) | 2018-09-03 | 2020-03-12 | Univerza V Ljubljani | New class of dna gyrase and/or topoisomerase iv inhibitors with activity against gram-positive and gram-negative bacteria |
EA202191349A1 (ru) | 2018-11-15 | 2021-08-10 | Ниппон Синяку Ко., Лтд. | 1,3,4-оксадиазолон и фармацевтический препарат |
WO2022129327A1 (en) | 2020-12-17 | 2022-06-23 | Univerza V Ljubljani | New n-phenylpyrrolamide inhibitors of dna gyrase and topoisomerase iv with antibacterial activity |
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IL23847A (en) | 1964-08-07 | 1969-02-27 | Merck & Co Inc | Benzimidazoles useful as antifungals |
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US5739135A (en) * | 1993-09-03 | 1998-04-14 | Bristol-Myers Squibb Company | Inhibitors of microsomal triglyceride transfer protein and method |
FR2766488B1 (fr) * | 1997-07-23 | 2000-02-18 | Hoechst Marion Roussel Inc | Nouveaux derives aromatiques substitues par un ribose, leur procede de preparation et leur application comme medicaments |
AU8673598A (en) * | 1997-08-01 | 1999-02-22 | University Of Florida | Neuraminidase inhibitors |
JP2003104971A (ja) | 1999-08-12 | 2003-04-09 | Wakunaga Pharmaceut Co Ltd | 新規アニリド誘導体又はその塩及びこれを含有する医薬 |
EP1251849A1 (de) | 2000-01-18 | 2002-10-30 | Vertex Pharmaceuticals Incorporated | Gyrase-inhibitoren und ihre verwendung |
EP1251848B1 (de) | 2000-01-18 | 2004-06-23 | Vertex Pharmaceuticals Incorporated | Gyrase-inhibitoren und ihre verwendung |
TWI284639B (en) | 2000-01-24 | 2007-08-01 | Shionogi & Co | A compound having thrombopoietin receptor agonistic effect |
AU2001269821A1 (en) | 2000-06-15 | 2001-12-24 | Barbara Chen | Cycloalkyl alkanoic acids as integrin receptor antagonists |
WO2002008224A1 (en) * | 2000-07-26 | 2002-01-31 | Smithkline Beecham P.L.C. | Aminopiperidine quinolines and their azaisosteric analogues with antibacterial activity |
US6964966B2 (en) | 2001-04-25 | 2005-11-15 | Wockhardt Limited | Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments |
DOP2002000386A (es) | 2001-05-30 | 2002-12-15 | Warner Lambert Co | Agentes antibacterianos |
IL160253A0 (en) | 2001-08-09 | 2004-07-25 | Ono Pharmaceutical Co | Carboxylic acid derivative compounds and drugs comprising these compounds as the active ingredient |
AU2002356689B2 (en) | 2001-12-05 | 2008-05-15 | Sanofi-Aventis Deutschland Gmbh | Substituted 4-phenyltetrahydroisoquinolines, method for the production thereof, the use thereof as medicaments, in addition to a medicament containing same |
AR038536A1 (es) | 2002-02-25 | 2005-01-19 | Upjohn Co | N-aril-2-oxazolidinona-5- carboxamidas y sus derivados |
US7183276B2 (en) | 2002-02-28 | 2007-02-27 | Takeda Pharmaceutical Company Limited | Azole compounds |
AR040336A1 (es) | 2002-06-26 | 2005-03-30 | Glaxo Group Ltd | Compuesto de piperidina, uso del mismo para la fabricacion de un medicamento, composicion farmaceutica que lo comprende y procedimiento para preparar dicho compuesto |
US7135469B2 (en) | 2003-03-18 | 2006-11-14 | Bristol Myers Squibb, Co. | Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors |
JPWO2004089954A1 (ja) | 2003-04-08 | 2006-07-06 | 大日本住友製薬株式会社 | 新規なカルバペネム化合物 |
DE10316081A1 (de) | 2003-04-08 | 2004-10-21 | Morphochem AG Aktiengesellschaft für kombinatorische Chemie | Neue Verbindungen mit antibakterieller Aktivität |
SE0302116D0 (sv) | 2003-07-21 | 2003-07-21 | Astrazeneca Ab | Novel compounds |
GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
US20050197336A1 (en) * | 2004-03-08 | 2005-09-08 | Miikana Therapeutics Corporation | Inhibitors of histone deacetylase |
US7345043B2 (en) * | 2004-04-01 | 2008-03-18 | Miikana Therapeutics | Inhibitors of histone deacetylase |
WO2006030975A1 (ja) | 2004-09-17 | 2006-03-23 | Takeda Pharmaceutical Company Limited | ピペリジン誘導体およびその用途 |
AU2005299501B2 (en) | 2004-10-22 | 2011-03-03 | Janssen Pharmaceutica N.V. | Aromatic amides as inhibitors of c-fms kinase |
HUE033089T2 (en) | 2004-10-22 | 2017-11-28 | Janssen Pharmaceutica Nv | C-FMS kinase inhibitors |
EP1856103A2 (de) | 2005-02-18 | 2007-11-21 | AstraZeneca AB | Pyrrolderivate als dna-gyrase- und topoisomeraseinhibitoren |
KR101422432B1 (ko) | 2005-02-18 | 2014-07-22 | 아스트라제네카 아베 | 항균성 피페리딘 유도체 |
JP2008530193A (ja) | 2005-02-18 | 2008-08-07 | アストラゼネカ アクチボラグ | 化合物 |
JP2008531671A (ja) | 2005-03-04 | 2008-08-14 | アストラゼネカ アクチボラグ | 化合物 |
JP2008531673A (ja) | 2005-03-04 | 2008-08-14 | アストラゼネカ アクチボラグ | 抗菌活性をもつアゼチジン及びピロールの三環式誘導体 |
CA2633563A1 (en) | 2005-12-23 | 2007-06-28 | Astrazeneca Ab | Antibacterial pyrrolopyridines, pyrrolopyrimidines, and pyrroloazepines |
-
2004
- 2004-09-09 TW TW093127317A patent/TW200526626A/zh unknown
- 2004-09-10 EP EP04768421A patent/EP1664025B1/de active Active
- 2004-09-10 AU AU2004272338A patent/AU2004272338B2/en not_active Expired - Fee Related
- 2004-09-10 ES ES04768421T patent/ES2291934T3/es active Active
- 2004-09-10 RU RU2006112046/04A patent/RU2006112046A/ru not_active Application Discontinuation
- 2004-09-10 US US10/571,212 patent/US7709503B2/en not_active Expired - Fee Related
- 2004-09-10 WO PCT/GB2004/003874 patent/WO2005026149A1/en active IP Right Grant
- 2004-09-10 CA CA002538552A patent/CA2538552A1/en not_active Abandoned
- 2004-09-10 KR KR1020067007045A patent/KR20070026318A/ko not_active Application Discontinuation
- 2004-09-10 BR BRPI0414330-2A patent/BRPI0414330A/pt not_active IP Right Cessation
- 2004-09-10 MX MXPA06002847A patent/MXPA06002847A/es unknown
- 2004-09-10 AT AT04768421T patent/ATE373650T1/de not_active IP Right Cessation
- 2004-09-10 DE DE602004009089T patent/DE602004009089T2/de active Active
- 2004-09-10 JP JP2006525891A patent/JP4959329B2/ja not_active Expired - Fee Related
- 2004-09-13 UY UY28510A patent/UY28510A1/es not_active Application Discontinuation
- 2004-09-13 AR ARP040103271A patent/AR046160A1/es not_active Application Discontinuation
-
2006
- 2006-03-07 IL IL174165A patent/IL174165A0/en unknown
- 2006-04-07 IS IS8403A patent/IS8403A/is unknown
- 2006-04-11 NO NO20061657A patent/NO20061657L/no not_active Application Discontinuation
- 2006-11-03 HK HK06112141A patent/HK1091491A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
AU2004272338A1 (en) | 2005-03-24 |
JP4959329B2 (ja) | 2012-06-20 |
DE602004009089T2 (de) | 2008-06-12 |
EP1664025B1 (de) | 2007-09-19 |
US20060223801A1 (en) | 2006-10-05 |
RU2006112046A (ru) | 2007-11-10 |
ES2291934T3 (es) | 2008-03-01 |
CA2538552A1 (en) | 2005-03-24 |
IL174165A0 (en) | 2006-08-01 |
ATE373650T1 (de) | 2007-10-15 |
JP2007505092A (ja) | 2007-03-08 |
TW200526626A (en) | 2005-08-16 |
HK1091491A1 (en) | 2007-01-19 |
KR20070026318A (ko) | 2007-03-08 |
MXPA06002847A (es) | 2006-06-14 |
AR046160A1 (es) | 2005-11-30 |
US7709503B2 (en) | 2010-05-04 |
EP1664025A1 (de) | 2006-06-07 |
UY28510A1 (es) | 2005-04-29 |
WO2005026149A1 (en) | 2005-03-24 |
IS8403A (is) | 2006-04-07 |
AU2004272338B2 (en) | 2008-06-05 |
BRPI0414330A (pt) | 2006-11-07 |
NO20061657L (no) | 2006-06-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8381 | Inventor (new situation) |
Inventor name: HAUCK, SHEILA IRENE, WALTHAM, MASSACHUSETTS 02, US Inventor name: HALES, NEIL JAMES, MACCLESFIELD, CHESHIRE SK10, GB Inventor name: NI, HAIHONG, WALTHAM, MASSACHUSETTS 02451, US Inventor name: HULL, KENNETH GREGORY, WALTHAM, MASSACHUSETTS , US Inventor name: MULLEN, GEORGE BYRON, WALTHAM, MASSACHUSETTS 0, US Inventor name: TIMMS, DAVID, MACCLESFIELD, CHESHIRE SK10 4TG, GB Inventor name: GREEN, OLUYINKA MORENIKE, WALTHAM, MASSACHUSET, US Inventor name: BREEZE, ALEXANDER LOUIS, MACCLESFIELD, CHESHIR, GB |
|
8364 | No opposition during term of opposition |